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内皮抑素联合化疗治疗小细胞肺癌的疗效与安全性:一项2期单臂多中心开放标签试验

Efficacy and safety of endostatin in combination with chemotherapy in small cell lung cancer: a phase 2 single-arm multicenter open-label trial.

作者信息

Zhao Yi, Zhang Xu, Jin Chenxing, Yu Xiaomin, Zhang Min, Cao Yang, Li Ying, Wang Aman, Shan Xiu, Zhang Jia, Wang Juhong, Yin Liu, Tan Xiaoxin, Liu Jiwei

机构信息

Department of Oncology, The First Affiliated Hospital of Dalian Medical University, Dalian, China.

The Clinical Skill Training Center of Dalian Medical University, Dalian, China.

出版信息

Ann Palliat Med. 2021 Mar;10(3):3277-3285. doi: 10.21037/apm-21-443.

Abstract

BACKGROUND

Small-cell lung cancer (SCLC) is a type of lung cancer with high invasiveness and poor prognosis. Although SCLC is effective for initial treatment, the vast majority of patients will relapse, the efficacy of posterior line therapy is limited, and there is a lack of effective treatment. At the same time, in the past 30 years, there has been little progress in first-line treatment. With the progress of antiangiogenic therapy, whether it can be used in the treatment of SCLC is worth exploring. Therefore, a single-arm multicenter clinical study was conducted on the efficacy, optimization, and safety of endostatin combined chemotherapy in SCLC.

METHODS

This study is a prospective non-blind single-arm multicenter study. From January 2016 to July 2019, a total of 22 patients with histologically diagnosed SCLC were enrolled in three centers. The treatment regimen was as follows: continuous intravenous pump infusion of endostatin (90 mg) for 72 hours, 3 days before chemotherapy, and continuous pump infusion of endostatin (120 mg) for 96 hours the next day following the infusion of chemotherapeutic drugs; the chemotherapy regimen was administered with standard platinum combined with etoposide once every 21 days. After six cycles, endostatin maintenance therapy was used until the disease progressed or intolerable adverse reactions occurred. The therapeutic effect was evaluated by imaging and oncology markers every two cycles, and the adverse reactions, tumor progression time, and patient survival time were recorded.

RESULTS

Among the 21 patients analyzed, the median progression-free survival (PFS) was 8.0 months, the median overall survival (OS) was 13.6 months, the objective effective rate (ORR) was 61.9%, and the disease control rate (DCR) was 95.2%. All patients tolerated the treatment. The main adverse reactions were myelosuppression, albuminuria, nausea, and vomiting. The incidence of grade 3 or 4 adverse reactions was 7.2%, which could be relieved by symptomatic support treatment. There were no treatment-related deaths.

CONCLUSIONS

Endostatin combined with platinum-etoposide is safe and effective in the treatment of SCLC.

摘要

背景

小细胞肺癌(SCLC)是一种侵袭性高、预后差的肺癌类型。尽管SCLC初始治疗有效,但绝大多数患者会复发,后线治疗疗效有限,且缺乏有效治疗方法。同时,在过去30年里,一线治疗进展甚微。随着抗血管生成治疗的进展,其是否可用于SCLC治疗值得探索。因此,开展了一项关于恩度联合化疗治疗SCLC的疗效、优化及安全性的单臂多中心临床研究。

方法

本研究为前瞻性非盲单臂多中心研究。2016年1月至2019年7月,三个中心共纳入22例经组织学确诊的SCLC患者。治疗方案如下:化疗前3天持续静脉泵入恩度(90mg)72小时,化疗药物输注次日持续泵入恩度(120mg)96小时;化疗方案为标准铂类联合依托泊苷,每21天给药一次。六个周期后,采用恩度维持治疗,直至疾病进展或出现无法耐受的不良反应。每两个周期通过影像学和肿瘤标志物评估治疗效果,并记录不良反应、肿瘤进展时间和患者生存时间。

结果

在分析的21例患者中,中位无进展生存期(PFS)为8.0个月,中位总生存期(OS)为13.6个月,客观有效率(ORR)为61.9%,疾病控制率(DCR)为95.2%。所有患者均耐受治疗。主要不良反应为骨髓抑制、蛋白尿、恶心和呕吐。3级或4级不良反应发生率为7.2%,经对症支持治疗可缓解。无治疗相关死亡。

结论

恩度联合铂类-依托泊苷治疗SCLC安全有效。

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